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Sense and anti-sense: Role of FAM83A and FAM83A-AS1 in Wnt, EGFR, PI3K, EMT pathways and tumor progression.

Authors :
Zhao, Chenshu
Li, Xiaowen
Zhang, Rui
Lyu, Hao
Xiao, Shuai
Guo, Dong
Ali, Declan William
Michalak, Marek
Chen, Xing-Zhen
Zhou, Cefan
Tang, Jingfeng
Source :
Biomedicine & Pharmacotherapy. Apr2024, Vol. 173, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

An increasing number of studies have shown that FAM83A, a member of the family with sequence similarity 83 (FAM83), which consists of eight members, is a key tumor therapeutic target involved in multiple signaling pathways. It has been reported that FAM83A plays essential roles in the regulation of Wnt/β-catenin, EGFR, MAPK, EMT, and other signaling pathways and physiological processes in models of pancreatic cancer, lung cancer, breast cancer, and other malignant tumors. Moreover, the expression of FAM83A could be significantly affected by multiple noncoding RNAs that are dysregulated in malignant tumors, the dysregulation of which is essential for the malignant process. Among these noncoding RNAs, the most noteworthy is the antisense long noncoding (Lnc) RNA of FAM83A itself (FAM83A-AS1), indicating an outstanding synergistic carcinogenic effect between FAM83A and FAM83A-AS1. In the present study, the specific mechanisms by which FAM83A and FAM83A-AS1 cofunction in the Wnt/β-catenin and EGFR signaling pathways were reviewed in detail, which will guide subsequent research. We also described the applications of FAM83A and FAM83A-AS1 in tumor therapy and provided a certain theoretical basis for subsequent drug target development and combination therapy strategies. [Display omitted] • FAM83A and FAM83A-AS1 regulates Wnt, EGFR, PI3K, and EMT signaling pathways. • FAM83A-AS1 enhance the mRNA stability of FAM83A directly. • FAM83A and FAM83A-AS1 effectively enhanced multiple types of cancers development. • Both FAM83A and FAM83A-AS1 represent promising therapeutic targets for cancers. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07533322
Volume :
173
Database :
Academic Search Index
Journal :
Biomedicine & Pharmacotherapy
Publication Type :
Academic Journal
Accession number :
176196445
Full Text :
https://doi.org/10.1016/j.biopha.2024.116372